Integra LifeSciences Corporation

60 total trials 3 currently recruiting 38 completed

Integra LifeSciences Corporation sponsors 60 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 38 completed. 5 of these trials are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Diabetic Foot Ulcer, with 2 trials.

Trial Pipeline

60 total, page 1 of 2

RECRUITING

AERA Pediatrics Registry

NCT07071298

RECRUITING NA

A Modified Platform Trial of Multiple CAMPs for the Management of Diabetic Foot Ulcers and Venous Leg Ulcers

NCT06453187

RECRUITING

The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation

NCT04494295

COMPLETED NA

MicroMatrix® Flex in Tunneling Wounds

NCT06629506

COMPLETED

Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health Study

NCT06297187

COMPLETED

T-GENVIH-003 LTFU (Long Term Follow Up) Study

NCT06034652

COMPLETED

Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair

NCT05610267

TERMINATED

REINVENT Registry (Registry of the Nerve Gap Repair From Integra)

NCT05339594

TERMINATED NA

NeuraGen 3D Pilot Study

NCT05343143

COMPLETED NA

The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of Intraventricular Hemorrhage (IVH)

NCT05113381

COMPLETED

Suturable DuraGen™ PMCF Study

NCT04923867

TERMINATED NA

Diabetic Foot Ulcer Study Comparing Cytal Wound Matrix 1-Layer to Standard of Care

NCT03626623

COMPLETED

Sundt™ Carotid Shunt Retrospective Post Market Clinical Follow-up Study (PMCF)

NCT03816202

TERMINATED

The Management of Pilonidal Wounds With ACell MicroMatrix® and Cytal® Wound Matrix: A Case Series

NCT04041037

TERMINATED

Cytal® Wound Matrix and MicroMatrix® Wound Study

NCT03632954

COMPLETED NA

AMNIOEXCEL® Plus vs A Marketed Comparator vs SOC in the Management of Diabetic Foot Ulcers

NCT03547635

COMPLETED NA

Comparing Concomitant Use of ACell MicroMatrix® and ACell Cytal™ to Standard of Care in Stage 3 or 4 Pressure Injuries

NCT03283787

COMPLETED NA

PriMatrix for the Management of Diabetic Foot Ulcers

NCT03010319

TERMINATED Phase 3

Open-Label Study in Diabetic Foot Ulcers (DFU), to Evaluate Safety of 0.03% DSC127 Topical Gel in Chronic Use

NCT01840085

TERMINATED NA

MEDIHONEY® Gel Versus Collagenase for Wound Debridement

NCT02482948

TERMINATED

Global Sinus Surgery Registry

NCT02347943

COMPLETED NA

Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers

NCT02209051

COMPLETED NA

ACell MatriStem Pelvic Floor Matrix Versus Native Tissue Repair, Comparative Study

NCT02021279

COMPLETED NA

Study of Safety and Efficacy for the Eustachian Tube Balloon Catheter

NCT02087150

COMPLETED

Retrospective Study Evaluating Outcomes for Integra® Skin Sheet Products in Lower Extremity Complex Wounds

NCT01947387

TERMINATED NA

A Comparative Efficacy Study: Treatment for Non-healing Diabetic Foot Ulcers

NCT01858545

TERMINATED Phase 3

Phase 3 Study Evaluating Efficacy and Safety of DSC127 Compared With Vehicle and With Standard-of-care in Diabetic Foot Ulcers

NCT01849965

TERMINATED Phase 3

Phase III Study to Evaluate Efficacy and Safety of DSC127 in Diabetic Foot Ulcers

NCT01830348

COMPLETED NA

Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)

NCT01714687

COMPLETED

Medical Therapy Versus Balloon Sinus Dilation for Patients With Chronic Rhinosinusitis

NCT01685229

TERMINATED NA

Health Economic Assessment of Lower Extremity Diabetic (HEALED) Ulcers With PriMatrix

NCT01729286

COMPLETED

Earset Healthy Volunteer Study

NCT01611246

COMPLETED NA

Tympanostomy Tube Placement in Children in the Office (Inova Study)

NCT01496287

COMPLETED NA

inVENT-visIOn Study

NCT01444391

COMPLETED

DuraSeal Exact Spine Sealant System Post-Approval Study

NCT01410864

COMPLETED

Healthy Volunteer Study

NCT01346332

COMPLETED NA

inVENT-In-Office Study

NCT01324271

TERMINATED NA

A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers

NCT01270633

COMPLETED Phase 2

Evaluation of the Tympanostomy Tube Delivery System

NCT01202578

COMPLETED

A Multicenter, Prospective, Observational Study With PriMatrix for the Treatment of Neuropathic Diabetic Foot Ulcers

NCT01228526

COMPLETED

Optimization and Refinement of Technique in In-Office Sinus Dilation 2

NCT01107379

COMPLETED NA

A Safety and Efficacy Study of INTEGRA® Dermal Regeneration Template for the Treatment of Diabetic Foot Ulcers

NCT01060670

COMPLETED NA

Acclarent Tympanostomy Tube Delivery System for the Treatment of Patients Requiring Tympanostomy Tube Insertion

NCT02150044

TERMINATED NA

An Evaluation of SprayShield in Reducing Post-Operative Adhesion Formation Following Major Open Abdominal Surgery

NCT01002287

COMPLETED NA

Anesthetizing the Tympanic Membrane in Healthy Volunteers

NCT01047904

COMPLETED

Large Abdominal Hernia Repair With SurgiMend 3.0

NCT00892333

COMPLETED NA

Clinical Study of the Tympanostomy Tube Delivery System

NCT00939796

COMPLETED NA

Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide

NCT00791934

TERMINATED Phase 3

PleuraSeal Pivotal Study (US)

NCT00748124

COMPLETED NA

Balloon Sinus Dilation In Office or OR

NCT00939393

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What the Pipeline for Integra LifeSciences Corporation Shows

According to the ClinicalTrials.gov registry, Integra LifeSciences Corporation is linked to 60 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 5% of the sponsor's indexed portfolio, and 38 are already marked complete, representing roughly 63% of the total.

The phase mix for Integra LifeSciences Corporation reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 1 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Integra LifeSciences Corporation is Diabetic Foot Ulcer with 2 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.